特发性肺纤维化急性加重期:治疗谁,如何治疗。

IF 1.1 Q4 RESPIRATORY SYSTEM Current pulmonology reports Pub Date : 2019-12-01 Epub Date: 2019-11-26 DOI:10.1007/s13665-019-00238-7
Tejaswini Kulkarni, Steven R Duncan
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引用次数: 4

摘要

综述目的:特发性肺纤维化急性加重(AE-IPF)是IPF患者最常见的死亡原因。在这里,我们回顾了AE-IPF的修订定义和诊断标准,并讨论了治疗策略,包括针对这种复杂综合征的机械靶向研究性治疗。最近的研究发现:最近报道了针对AE-IPF涉及的炎症、自身免疫和凝血级联等多种途径的新疗法。虽然这些报告大多是小规模和非对照的,但它们为设计更大规模的随机、对照、多中心研究提供了证据,以改善AE-IPF患者的预后。总结:AE-IPF预后不佳,目前的治疗主要包括支持性护理和症状缓解。目前对AE-IPF的治疗方法(包括皮质类固醇)缺乏共识,但目前针对新治疗策略的随机对照研究可能会带来希望。
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Acute exacerbation of idiopathic pulmonary fibrosis: who to treat, how to treat.

Purpose of review: Acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF) are the most frequent cause of death among patients with IPF. Here, we review the revised definition and diagnostic criteria for AE-IPF and discuss management strategies including mechanistically targeted investigational therapies for this complex syndrome.

Recent findings: Novel therapies targeting various pathways including inflammation, autoimmunity and coagulation cascade involved in AE-IPF have recently been reported. Although most of these reports are small and uncontrolled, they have provided evidence to design larger randomized, controlled, multicenter studies to improve outcomes among patients with AE-IPF.

Summary: AE-IPF has a dismal prognosis and current treatment consists mainly of supportive care and symptom palliation. There is a lack of consensus on current therapies for AE-IPF, including corticosteroids, but current randomized control studies for newer therapeutic strategies may hold promise.

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